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Journal Abstract Search

218 related items for PubMed ID: 10899455

  • 21.
    ; . PubMed ID:
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  • 22.
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  • 23. Screening of common mitochondrial mutations in Chinese patients with mitochondrial encephalomyopathies.
    Qi Y, Zhang Y, Wang Z, Yang Y, Yuan Y, Niu S, Pei P, Wang S, Ma Y, Bu D, Zou L, Fang F, Xiao J, Sun F, Zhang Y, Wu Y, Wang S, Xiong H, Wu X.
    Mitochondrion; 2007; 7(1-2):147-50. PubMed ID: 17276742
    [Abstract] [Full Text] [Related]

  • 24. 174th ENMC international workshop: Applying pre-implantation genetic diagnosis to mtDNA diseases: implications of scientific advances 19-21 March 2010, Naarden, The Netherlands.
    Poulton J, Bredenoord AL.
    Neuromuscul Disord; 2010 Aug; 20(8):559-63. PubMed ID: 20627569
    [No Abstract] [Full Text] [Related]

  • 25. 52nd ENMC International Workshop: International Consortium on Nucleo-mitochondrial Interactions. 4-6 July 1997, Naarden, The Netherlands.
    Neuromuscul Disord; 1998 Feb; 8(1):57-8. PubMed ID: 9565993
    [No Abstract] [Full Text] [Related]

  • 26. Mitochondrial DNA polymorphism in disease: a possible contributor to respiratory dysfunction.
    Lertrit P, Kapsa RM, Jean-Francois MJ, Thyagarajan D, Noer AS, Marzuki S, Byrne E.
    Hum Mol Genet; 1994 Nov; 3(11):1973-81. PubMed ID: 7874114
    [Abstract] [Full Text] [Related]

  • 27. Clinical features associated with the A-->G transition at nucleotide 8344 of mtDNA ("MERRF mutation").
    Silvestri G, Ciafaloni E, Santorelli FM, Shanske S, Servidei S, Graf WD, Sumi M, DiMauro S.
    Neurology; 1993 Jun; 43(6):1200-6. PubMed ID: 8170567
    [Abstract] [Full Text] [Related]

  • 28. A rapid and sensitive PCR screening method for point mutations associated with mitochondrial encephalomyopathies.
    Seibel P, Flierl A, Kottlors M, Reichmann H.
    Biochem Biophys Res Commun; 1994 Apr 29; 200(2):938-42. PubMed ID: 8179630
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  • 29.
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  • 30. A MELAS/MERRF phenotype associated with the mitochondrial DNA 5521G>A mutation.
    Herrero-Martín MD, Ayuso T, Tuñón MT, Martín MA, Ruiz-Pesini E, Montoya J.
    J Neurol Neurosurg Psychiatry; 2010 Apr 29; 81(4):471-2. PubMed ID: 20360171
    [No Abstract] [Full Text] [Related]

  • 31.
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  • 32. [Diagnosis and therapy of mitochondriopathies].
    Sperl W.
    Wien Klin Wochenschr; 1997 Feb 14; 109(3):93-9. PubMed ID: 9139466
    [Abstract] [Full Text] [Related]

  • 33.
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  • 34.
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  • 35. Inheritance and expression of mitochondrial DNA point mutations.
    Holme E, Tulinius MH, Larsson NG, Oldfors A.
    Biochim Biophys Acta; 1995 May 24; 1271(1):249-52. PubMed ID: 7599216
    [Abstract] [Full Text] [Related]

  • 36. The mitochondrial DNA 10197 G > A mutation causes MELAS/Leigh overlap syndrome presenting with acute auditory agnosia.
    Leng Y, Liu Y, Fang X, Li Y, Yu L, Yuan Y, Wang Z.
    Mitochondrial DNA; 2015 Apr 24; 26(2):208-12. PubMed ID: 24708134
    [Abstract] [Full Text] [Related]

  • 37. The 3243 MELAS mutation in a pedigree with MERRF.
    Folgerø T, Torbergsen T, Oian P.
    Eur Neurol; 1995 Apr 24; 35(3):168-71. PubMed ID: 7628497
    [Abstract] [Full Text] [Related]

  • 38. MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes.
    Nakamura M, Yabe I, Sudo A, Hosoki K, Yaguchi H, Saitoh S, Sasaki H.
    J Med Genet; 2010 Oct 24; 47(10):659-64. PubMed ID: 20610441
    [Abstract] [Full Text] [Related]

  • 39. Mitochondrial gene mutations and human diseases: a prolegomenon.
    Howell N.
    Am J Hum Genet; 1994 Aug 24; 55(2):219-24. PubMed ID: 8037201
    [No Abstract] [Full Text] [Related]

  • 40. [Mitochondrial myopathy, deafness and type 2 diabetes mellitus with tRNALeu(UUR) point mutation in mitochondrial DNA].
    Stratilová L, Zeman J, Hansíková H, Houstĕk J, Hermanská J, Dudková Z, Konrádová V, Hůlková H, Elleder M.
    Cas Lek Cesk; 1998 Jul 13; 137(14):430-3. PubMed ID: 9748738
    [Abstract] [Full Text] [Related]

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